Production Technician I - ILP 3rd Shift

Quva•Sugar Land, TX

1d•Onsite

About The Position

The Production Technician I – ILP supports product visual inspection, labeling, and packaging operations at Quva’s facility, following established processes and procedures. The role contributes to producing medications that meet safety, efficacy, and quality standards. It is a full-time, onsite position at the Sugar Land location, working a consistent Monday–Friday 3rd-shift schedule from 10:00 PM to 6:30 AM CST. Minimum overtime requirements apply. This safety-sensitive position may be subject to random drug testing in accordance with applicable laws.

Requirements

High school diploma or GED from a recognized institution or organization.
Pass a color perception exam.
Pass a vision exam demonstrating 20/20 vision with or without correction.
Successfully complete a drug and background check.
Be at least 18 years old.
Be currently authorized to work in the United States on a full-time basis; Quva will not sponsor work visas.
Demonstrate strong attention to detail, communication skills, and the ability to work effectively with people across departments and organizational levels.
Follow policies and procedures and complete administrative tasks correctly and on time.
Adapt to support multiple production areas and shifts as needed.

Nice To Haves

Pharmaceutical experience.
Mechanical aptitude.
Working knowledge of cGMPs, regulatory requirements, and applicable SOPs.

Responsibilities

Assist with preparing materials and supplies for inspection and packaging rooms.
Label and process production materials as required.
Clean rooms and equipment daily, bi-weekly, or monthly, and complete applicable preventive maintenance forms and checklists in accordance with SOPs.
Conduct and complete line and room clearances according to established procedures.
Complete documents required for product accountability and traceability, following Good Documentation Practices (GDPs), cGMPs, and company ISO standards.
Comply with 503B guidelines, cGMPs, standard operating procedures, and company policies.
Perform equipment calibration checks and troubleshoot production equipment as needed.
Document activities according to established procedures.
Immediately notify production management of deviations from established processes or procedures.
Assist other areas as needed, including cleaning, non-sterile filling, kitting, and preparation operations.
Perform primary, secondary, and tertiary product labeling.
Perform secondary and final product packaging.
Visually inspect products.
Maintain an inspection-ready environment and support internal and external audits.